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The timing of administration of a steroid, dexamethasone, on the postoperative relief from pain in women undergoing uterus removal surgery.

Not Applicable
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2021/02/031024
Lead Sponsor
Dr Premangshu Ghoshal
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients undergoing open total abdominal hysterectomy under spinal anaesthesia

Exclusion Criteria

Refusal to give consent,

Known history of Corticosteroid hypersensitivity,

Diabetes Mellitus patients,

Increased Preoperative TLC Count,

Patients already receiving corticosteroid or immunosuppresive drugs preoperatively,

Previous history of gastric ulcer,

Receiving other analgesics,

Patients for whom general anesthesia will be required because of unexpectedly prolonged surgery for any reason or because of any complication

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
VASTimepoint: 6 hours
Secondary Outcome Measures
NameTimeMethod
24 hour incidence of PONVTimepoint: Upto 24 hours post-operatively;Cumulative 24 hours Opioid UseTimepoint: Upto 24 hours post-operatively;Difference in VASTimepoint: 24 hours;Duration of post-operative hospital stay in daysTimepoint: Until hospital discharge;Duration of stay in recovery unitTimepoint: Upto 6 hours post-operatively;Incidence of any wound infectionTimepoint: Until hospital discharge;Time in minutes to request for first analgesicTimepoint: Upto 8 hours post-operatively;Time to passage of faecesTimepoint: Until hospital discharge;Time to regression of motor blockade by Modified Bromage Scale and sensory blockade to 2 dermatomal levelsTimepoint: Upto 4 hours post-operatively
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